what are risk assement in the analytical qbd?

why multimedia dissolution require to do?

in OSD forms require to use gas chromatography?

why require to do water content for drug product?

before starting analytical method valodation what you checking? and how giving preference to start validation?

in which situation ion pair agent require to use?

effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?

if you given one product then which tests you will perform?

on the basis of bcs class how to proceed the solubility?

for which product require to do content uniformity? what is limit of cu?

how require to select dissolution media? what is discrimination?

if rsd failed then what require to do?

if peak get problamatic then what require to do?

how you confirm the assay method?

why cone formation during dissolution?